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柯萨奇病毒 B4 诱导的急性心肌炎和大脑皮质神经元水肿的鼠模型。

Murine model of acute myocarditis and cerebral cortical neuron edema induced by coxsackievirus B4.

机构信息

Key Laboratory of Etiology and Epidemiology of Emerging Infectious Diseases in Universities of Shandong, Taishan Medical University, Taian Shandong 271000, China.

Shanghai Jinshan Center for Disease Control and Prevention, Shanghai 201599, China.

出版信息

Zool Res. 2018 Jan 18;39(1):52-57. doi: 10.24272/j.issn.2095-8137.2017.056.

Abstract

Globally, coxsackievirus B4 (CV-B4) has been continuously isolated and evidence suggests an association with the development of pancreatitis and type I diabetes. In addition, CV-B4 is also associated with myocarditis and severe central nervous system (CNS) complications, which remain poorly studied and understood. In the present study, we established an Institute for Cancer Research (ICR) mouse model of CV-B4 infection and examined whether CV-B4 infection resulted in a predisposition to myocarditis and CNS infection. We found high survival in both the treatment and control group, with no significant differences in clinical outcomes observed. However, pathological lesions were evident in both brain and heart tissue of the CV-B4-infected mice. In addition, high viral loads were found in the neural and cardiac tissues as early as 2 days post infection. Expressions of IFN-γ and IL-6 in sera were significantly higher in CV-B4-infected mice compared to uninfected negative controls, suggesting the involvement of these cytokines in the development of histopathological lesions. Our murine model successfully reproduced the acute myocarditis and cerebral cortical neuron edema induced by CV-B4, and may be useful for the evaluation of vaccine candidates and potential antivirals against CV-B4 infection.

摘要

全球范围内,柯萨奇病毒 B4(CV-B4)持续被分离出来,有证据表明其与胰腺炎和 1 型糖尿病的发展有关。此外,CV-B4 还与心肌炎和严重的中枢神经系统(CNS)并发症有关,但这些方面的研究和了解仍不够充分。在本研究中,我们建立了一个柯萨奇病毒 B4 感染的 ICR 小鼠模型,并研究了 CV-B4 感染是否导致心肌炎和 CNS 感染的易感性。我们发现治疗组和对照组的存活率都很高,临床结果没有明显差异。然而,CV-B4 感染的小鼠的脑组织和心脏组织都出现了明显的病理损伤。此外,在感染后 2 天,神经和心脏组织中就已经检测到高病毒载量。与未感染的阴性对照组相比,CV-B4 感染的小鼠血清中的 IFN-γ 和 IL-6 表达显著升高,表明这些细胞因子参与了组织病理学损伤的发生。我们的小鼠模型成功复制了 CV-B4 引起的急性心肌炎和大脑皮质神经元水肿,可能有助于评估 CV-B4 感染的疫苗候选物和潜在的抗病毒药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37a3/5869242/107eba1b49ab/ZoolRes-39-1-52-g001.jpg

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